Cyproheptadine Hydrochloride 70752-0101
Product NDC
70752-0101- Manufacturer
- Quagen Pharmaceuticals Llc
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 22, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA212423
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cyproheptadine Hydrochloride | 2 mg/5mL |
Packaging Options(1)
473 mL in 1 BOTTLE, GLASS (70752-101-12)